반응 #355087

ord-4014441c959c4f328c51cdce42c99f78

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출extracted with chloroform
  2. 2
    세척The chloroform solution is washed with 10% sodium bicarbonate solution
  3. 3
    기타dried
  4. 4
    기타evaporated in vacuo
  5. 5
    기타to give an oily residue
  6. 6
    기타chromatographed on a 40 g-silica gel column
  7. 7
    세척Elution with chloroform
  8. 8
    기타gives 400 mg of slightly impure product
  9. 9
    기타The 990 mg is recrystallized twice from acetone-hexane

실험 절차

A solution of 1.54 g of 9-fluoro-11β ,17,21-trihydroxy-16α-[(2-methyl-oxiranyl)methoxy]pregn-4-ene-3,20-dione, 21-acetate in 50 ml of tetrahydrofuran is stirred for 270 minutes with a solution of 2.6 g of periodic acid in 20 ml of water. The solution is poured into water and extracted with chloroform. The chloroform solution is washed with 10% sodium bicarbonate solution, dried, and evaporated in vacuo to give an oily residue. This is dissolved in chloroform and chromatographed on a 40 g-silica gel column. Elution with chloroform gives 400 mg of slightly impure product followed by 990 mg of TLC homogeneous solid. The 990 mg is recrystallized twice from acetone-hexane to give 328 mg of 9-fluoro-11β ,17,21-trihydroxy-16α-(2-oxopropoxy)pregn-4-ene-3,20-dione, 21-acetate, melting point 203°-208°C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US03945997uspto-grants-1976_03